| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000308696 |
| Start |
231146342:231146342(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2101A>C |
| AA Mutation |
p.Ile701Leu(p.I701L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000308696 |
| Start |
231062509:231062509(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.138G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000308696 |
| Start |
231166002:231166002(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs149102064
|
| CDS Mutation |
c.2700C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |